HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1991225Erstellt: 26. Oktober 2026
Benzimidazole → 2-(1H-benzimidazol-1-yl)-N-[3-(trifluoromethyl)phenyl]acetamide
https://huagongshe.com/reaction/1991225
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Benzimidazole | HCID 5798 | — |
| Edukt | 2-bromo-N-[3-(trifluoromethyl)phenyl]acetamide | HCID 2317152 | — |
| Edukt | Potassium tert-butoxide | HCID 23665647 | — |
| Produkt | 2-(1H-benzimidazol-1-yl)-N-[3-(trifluoromethyl)phenyl]acetamide | HCID 744841 | 27% |
Reaktionsschritte
A solution of potassium tert-butoxide (1.7 mL of 1 M solution in THF, 1.7 mmol,) was added to a solution of 1H-benzoimidazole (165 mg, 1.4 mmol) in anhydrous TBF (3 mL). The reaction mixture was stirred for 20 min at ambient temperature. 2-Bromo-N-(3-trifluoromethyl-phenyl)-acetamide (Example 92 part A) was added (261 mg, 0.93 mmol) and the mixture was stirred at 55° C. for subsequent 24 h. The crude product was purified on a preparative HPLC (XTerra C8 column 19×300 mm, 0.1 M aqueous NH4Ac/CH3CN). The pooled fractions were lyophilized to afford 81 mg (27%) of the title compound. Calculated for C16H12F3N3O m/z: 319.29, found 320.0 [M+H]+. 1H NMR (400 MeOH) δ ppm 5.2 (s, 2H), 7.3 (m, 2H), 7.4 (d, J=7.6 Hz, 1H), 7.5 (m, 2H), 7.7 (d,J=7.1 Hz, 1H), 7.8 (d, J=8.6 Hz, 1H), 8.0 (s, 1H), 8.2 (s, 1H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07645784B2 |
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| Quelldatensatz | uspto-grants-2010_01 |
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| ORD ID | ord-110f99951c78407bb9d7bc1f01e3d192 |
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| Quellennotiz | uspto-grants-2010_01 |
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